Medical Electronic Record Exchange
Country not established
- Devices
- 1
What Medical Electronic Record Exchange makes
The company manufactures the MXT-2, a 12-lead micro-transmitter designed for transmitting electrocardiogram (ECG) data wirelessly from portable monitoring devices to central systems for diagnostic review.
This device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Mxt-2 12 Lead Micro-Transmitter Ref K933012
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Electronic Record Exchange have in the registry?
The registry currently lists 1 device for Medical Electronic Record Exchange. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Electronic Record Exchange's devices?
Among its 1 most recently registered device, Medical Electronic Record Exchange has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Electronic Record Exchange's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Electronic Record Exchange's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Electronic Record Exchange in the registry?
The most recently registered devices listed for Medical Electronic Record Exchange include MXT-2 12 LEAD MICRO-TRANSMITTER.